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Challenges in the orthodontic treatment of a patient with pycnodysostosis

机译:正畸牙列固定术患者的正畸治疗中的挑战

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摘要

Pycnodysostosis is a rare, autosomal recessive syndrome characterized by osteosclerosis, brittle bones, stunting, and significant craniofacial changes. The objective of this study was to report a case of a 6-year-old patient with pycnodysostosis orthodontically treated and followed up until age 10 years and to discuss the risk factors, options for orthodontic treatment, and limitations involving this type of treatment, which has not yet been performed. Prevention through counseling and periodic follow-up visits is essential in eliminating factors that predispose patients to infections and fractures. New studies are necessary to establish safe and efficient orthodontic treatment plans.
机译:碧萝ody(Pycnodysostosis)是一种罕见的常染色体隐性遗传综合征,其特征为骨硬化,骨骼脆,发育迟缓和明显的颅面变化。这项研究的目的是报告一名正畸治疗并持续随访至10岁的6岁幽门突突症患者的病例,并讨论其危险因素,正畸治疗选择以及涉及此类治疗的局限性,尚未执行。通过咨询和定期随访访问进行的预防对于消除使患者容易感染和骨折的因素至关重要。建立安全有效的正畸治疗计划必须进行新的研究。

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